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Trial registered on ANZCTR
Registration number
ACTRN12610000758000
Ethics application status
Approved
Date submitted
16/05/2010
Date registered
14/09/2010
Date last updated
14/09/2010
Type of registration
Retrospectively registered
Titles & IDs
Public title
The effect of exercises using equipment in conjunction with an arm sleeve compression to reduce the size of lymphedematous in patients after breast cancer
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Scientific title
The effect of exercises utilizing apparatus associated with an arm sleeve compression garment on reducing the size of lymphedematous in patients after breast cancer
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Secondary ID [1]
251778
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Null
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Condition: Lymphedema
257374
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Condiction: Breast Cancer
257385
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Condition category
Condition code
Physical Medicine / Rehabilitation
257520
257520
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0
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Occupational therapy
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Cardiovascular
257521
257521
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0
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Diseases of the vasculature and circulation including the lymphatic system
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Cancer
257533
257533
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0
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Breast
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
The study will examine the effectiveness reduction in the size of lymphedematous arms of patients after breast cancer with a difference in volume of 200 mL between arm compared with the normal arm, diagnostic criterion(clinical) for lymphedema ,utilizing a facilitating exercising device associated with a compression arm sleeve. The compression used is made national material -polyester and cotton, low elasticity (>15mmHg) involving whole member (arm and forearm), put immediately prior to activity. The patients will submitted to a single one-hour session of active exercises, while sitting with the spinal column erect, of four 12-minute stints with intervals of three minutes to rest. Evaluation was achieved by water volumetry before and immediately after the session. The active exercising device is similar to the pedaling system of a bicycle that utilizes both upper limbs. This apparatus is fixed on a table at a height of 30 cm with the table at a distance of 10 cm from the patient's body.
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Intervention code [1]
256481
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Rehabilitation
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Intervention code [2]
256491
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Treatment: Devices
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Comparator / control treatment
No have control group, the control is upper limb healthy(volume).
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Reduction in the volume of the lymphedematous arms of patients utilizing a facilitating exercising device associated with a compression arm sleeve after one hour the activity. Evaluation will achieved by water volumetry before and immediately after the session.The volume of lymphedematous arm and healthy upper arm will be evaluated initial and after activity to compare the reduction (control).
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Assessment method [1]
258435
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Timepoint [1]
258435
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Funcional evaluation: The primary outcome is to evaluate the volume inicial the limbs for volumetry before beginning the proposed activity and assess immediately after an hour of activity.
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Secondary outcome [1]
264218
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Nill
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Assessment method [1]
264218
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Timepoint [1]
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Nill
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Eligibility
Key inclusion criteria
Lymphedema patients after breast cancer
Patients undergoing treatment will require written permission from their physician
Without active infection and skin lesion
Patients must sign a consent form to participate
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Minimum age
20
Years
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Maximum age
90
Years
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Sex
Females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Patients undergoing treatment without physician's written permission
Patients with active infection and skin lesion
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Nill
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Nill
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Single group
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Safety/efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
15/05/2010
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
30
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
2629
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Brazil
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State/province [1]
2629
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Funding & Sponsors
Funding source category [1]
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Government body
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Name [1]
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CAPES-Coordination of Improvement of Personal of Superior Level -Brazil
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Address [1]
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Setor Bancario Norte, Quadra 2, Bloco L, Lote 06, CEP 70040-020 - Brasilia, DF
Brazil
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Country [1]
256972
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Brazil
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Primary sponsor type
Government body
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Name
CAPES-Coordination of Improvement of Personal of Superior Level -Brazil
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Address
Setor Bancario Norte, Quadra 2, Bloco L, Lote 06, CEP 70040-020 - Brasilia, DF
Brazil
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Country
Brazil
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
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Country [1]
256233
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Other collaborator category [1]
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University
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Name [1]
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Medicine School of Sao Jose do Rio Preto
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Address [1]
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AV Brigadeiro Faria Lima 5416
Sao Jose do Rio Preto-SP-Brazil
CEP:15090-000
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Country [1]
251490
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Brazil
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
258987
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Committee Ethics Instituto de Biociencias Letras e Ciencias Exatas, Campus de Sao Jose do Rio Preto - SP
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Ethics committee address [1]
258987
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Rua Cristovao Colombo, 2265 Bairro: Jardim Nazareth CEP: 15054-000 Sao Jose do Rio Preto - Sao Paulo
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Ethics committee country [1]
258987
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Brazil
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Date submitted for ethics approval [1]
258987
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13/02/2007
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Approval date [1]
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12/03/2007
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Ethics approval number [1]
258987
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1/11/2007
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Summary
Brief summary
Aim: The aim of this study will to evaluate the reduction in the size of lymphedematous arms of patients utilizing a facilitating exercising device associated with a compression arm sleeve. Methods: Thirty subjects, suffering from arm lymphedema after surgical, chemotherapeutic and radiotherapeutic treatment for breast cancer. The criterion for starting the assessments will be by finishing order of subjects in a rehabilitation group. The patients were submitted to a one-hour session of active exercises, while sitting with the spinal column erect, of four 12-minute stints with intervals of three minutes to rest. Evaluation will achieved by water volumetry before and immediately after the session. The active exercising device is similar to the pedaling system of a bicycle. The paired t-test will employed for statistical analysis with an alpha error of 5% (p-value < 0.05) being considered acceptable.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Address
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Country
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Phone
31167
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Fax
31167
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Email
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Contact person for public queries
Name
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Jose Maria Pereira de Godoy
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Address
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Rua Floriano Peixoto 2950
Sao Jose do Rio Preto-Sao Paulo-Brazil
Zipe code:15020010
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Country
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Brazil
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Phone
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Phone: 55 17 32326362
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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Maria de Fatima Guerreiro Godoy
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Address
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Rua Floriano Peixoto 2950
Sao Jose do Rio Preto-Sao Paulo-Brazil
Zipe code:15020010
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Country
5342
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Brazil
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Phone
5342
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Phone: 55 17 32326362
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Fax
5342
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Email
5342
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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